Gestri Gaia, Carl Matthias, Appolloni Irene, Wilson Stephen W, Barsacchi Giuseppina, Andreazzoli Massimiliano
Sezione di Biologia Cellulare e dello Sviluppo, Dipartimento di Fisiologia, e Biochimica, Universita' degli Studi di Pisa, Via Carducci 13, 56010 Ghezzano (Pisa), Italy.
Development. 2005 May;132(10):2401-13. doi: 10.1242/dev.01814. Epub 2005 Apr 20.
Although it is well established that Six3 is a crucial regulator of vertebrate eye and forebrain development, it is unknown whether this homeodomain protein has a role in the initial specification of the anterior neural plate. In this study, we show that exogenous Six3 can expand the anterior neural plate in both Xenopus and zebrafish, and that this occurs in part through Six3-dependent transcriptional regulation of the cell cycle regulators cyclinD1 and p27Xic1, as well as the anti-neurogenic genes Zic2 and Xhairy2. However, Six3 can still expand the neural plate in the presence of cell cycle inhibitors and we show that this is likely to be due to its ability to repress the expression of Bmp4 in ectoderm adjacent to the anterior neural plate. Furthermore, exogenous Six3 is able to restore the size of the anterior neural plate in chordino mutant zebrafish, indicating that it has the ability to promote anterior neural development by antagonising the activity of the BMP pathway. On its own, Six3 is unable to induce neural tissue in animal caps, but it can do so in combination with Otx2. These results suggest a very early role for Six3 in specification of the anterior neural plate, through the regulation of cell proliferation and the inhibition of BMP signalling.
尽管Six3作为脊椎动物眼睛和前脑发育的关键调节因子已被广泛认可,但尚不清楚这种同源结构域蛋白在前神经板的初始特化过程中是否发挥作用。在本研究中,我们发现外源性Six3可在非洲爪蟾和斑马鱼中扩大前神经板,这部分是通过Six3依赖的细胞周期调节因子细胞周期蛋白D1和p27Xic1以及抗神经源性基因Zic2和Xhairy2的转录调控实现的。然而,在存在细胞周期抑制剂的情况下,Six3仍能扩大神经板,我们发现这可能是由于其抑制前神经板相邻外胚层中Bmp4表达的能力。此外,外源性Six3能够恢复chordino突变斑马鱼前神经板的大小,表明它具有通过拮抗BMP信号通路的活性来促进前神经发育的能力。单独的Six3无法在动物帽中诱导神经组织,但它与Otx2联合时则可以。这些结果表明,Six3通过调节细胞增殖和抑制BMP信号,在前神经板特化过程中发挥非常早期的作用。